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The Neurospora crassa Genome: Cosmid Libraries Sorted by Chromosome

机译:Neurospora crassa基因组:粘粒库按染色体排序

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A Neurospora crassa cosmid library of 12,000 clones (at least nine genome equivalents) has been created using an improved cosmid vector pLorist6Xh, which contains a bacteriophage λ origin of replication for low-copy-number replication in bacteria and the hygromycin phosphotransferase marker for direct selection in fungi. The electrophoretic karyotype of the seven chromosomes comprising the 42.9-Mb N. crassa genome was resolved using two translocation strains. Using gel-purified chromosomal DNAs as probes against the new cosmid library and the commonly used medium-copy-number pMOcosX N. crassa cosmid library in two independent screenings, the cosmids were assigned to chromosomes. Assignments of cosmids to linkage groups on the basis of the genetic map vs. the electrophoretic karyotype are 93 ± 3% concordant. The size of each chromosome-specific subcollection of cosmids was found to be linearly proportional to the size of the particular chromosome. Sequencing of an entire cosmid containing the qa gene cluster indicated a gene density of 1 gene per 4 kbp; by extrapolation, 11,000 genes would be expected to be present in the N. crassa genome. By hybridizing 79 nonoverlapping cosmids with an average insert size of 34 kbp against cDNA arrays, the density of previously characterized expressed sequence tags (ESTs) was found to be slightly 1 per cosmid ( i.e. , 1 per 40 kbp), and most cosmids, on average, contained an identified N. crassa gene sequence as a starting point for gene identification.
机译:使用改良的粘粒载体pLorist6Xh创建了12,000个克隆的Neurospora crassa粘粒文库(至少9个基因组当量),该质粒包含噬菌体λ复制起点,用于细菌中的低拷贝数复制和潮霉素磷酸转移酶标记物,可直接选择在真菌中。使用两个易位菌株解析了包含42.9-Mb crassa的7条染色体的电泳核型。在两次独立筛选中,使用凝胶纯化的染色体DNA作为针对新粘粒文库的探针和常用的中等拷贝数pMOcosX N. crassa粘粒文库,将这些粘粒分配给了染色体。根据遗传图谱和电泳核型,将粘粒分配给连接基团的一致性为93±3%。发现粘粒的每个染色体特定亚群的大小与特定染色体的大小成线性比例。对包含qa基因簇的整个粘粒进行测序表明,其基因密度为每4 kbp 1个基因。通过外推法,预计N. crassa基因组中将存在11,000个基因。通过将79个平均插入片段大小为34 kbp的非重叠粘粒与cDNA阵列杂交,发现先前表征的表达序列标签(EST)的密度略小于每个粘粒1(即,每40 kbp 1个),而大多数粘粒,平均而言,含有鉴定出的克雷萨猪笼草基因序列作为基因鉴定的起点。

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